NCT07485790

Brief Summary

It is thought that a yoga intervention administered to pregnant women will reduce stress levels, enhance sexual quality of life, and positively affect sleep habits. According to the power analysis results, the study must include at least 70 pregnant women (35 in the experimental group and 35 in the control group). Data will be collected through a Personal Information Form, the Perceived Stress Scale (PSS), the Sexual Quality of Life Questionnaire-Female (SQLQ-F), and a Sleep Habits Form. In this study, the yoga practice will be administered to the pregnant women in the experimental group by the researcher.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
4mo left

Started Mar 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress41%
Mar 2026Sep 2026

Study Start

First participant enrolled

March 15, 2026

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

March 17, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

March 20, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2026

Last Updated

March 20, 2026

Status Verified

March 1, 2026

Enrollment Period

5 months

First QC Date

March 17, 2026

Last Update Submit

March 17, 2026

Conditions

Keywords

sexual quality of lifepregnant womenyoga

Outcome Measures

Primary Outcomes (1)

  • Perceived Stress Scale (PSS)

    The minimum score that can be obtained from the scale is "0", the maximum score is "32", and as the score obtained from the scale increases, stress levels also increase.

    At the end of the 6 weeks

Secondary Outcomes (2)

  • Sexual Quality of Life Questionnaire-Female (SQLQ-F)

    At the end of the 6 weeks

  • Sleep Habits

    At the end of the 6 weeks

Study Arms (2)

Experimental group

EXPERIMENTAL

Yoga

Behavioral: Yoga

Control group

NO INTERVENTION

Control group

Interventions

YogaBEHAVIORAL

Prenatal yoga training is designed taking into account the physiological and psychological changes of pregnancy. The training includes low-risk and pregnancy-appropriate yoga practices that prioritize the safety of pregnant women.

Experimental group

Eligibility Criteria

Age18 Years+
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsPregnant women
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • In their third trimester,
  • Able to read and write in Turkish,
  • Use a smartphone and have internet access,
  • Have no communication barriers,
  • Voluntarily agree to participate in the research.

You may not qualify if:

  • Pregnant women with any risk factors during pregnancy,
  • Pregnant women with any chronic illness,
  • Pregnant women with a diagnosed psychological problem,
  • Pregnant women with any exercise restrictions imposed by a physician,
  • Pregnant women participating in a different training program (meditation, relaxation, etc.)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Amasya University

Amasya, 05000, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Sleep Wake Disorders

Interventions

Yoga

Condition Hierarchy (Ancestors)

Nervous System DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsMental Disorders

Intervention Hierarchy (Ancestors)

Mind-Body TherapiesComplementary TherapiesTherapeuticsSpiritual TherapiesExercise Movement TechniquesPhysical Therapy Modalities

Study Officials

  • Emine İbici Akça, PhD

    Amasya University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Emine İbici Akça, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 17, 2026

First Posted

March 20, 2026

Study Start

March 15, 2026

Primary Completion (Estimated)

August 1, 2026

Study Completion (Estimated)

September 1, 2026

Last Updated

March 20, 2026

Record last verified: 2026-03

Locations